Karimnia Nazanin, Wilson Amy L, Doran Brittany R, Do Jennie, Matthews Amelia, Ho Gwo Y, Plebanski Magdalena, Jobling Thomas W, Stephens Andrew N, Bilandzic Maree
Hudson Institute of Medical Research, 27-31 Wright St, Clayton, VIC, 3168, Australia.
Department of Molecular and Translational Sciences, Monash University, 45 Kanooka Grove, Clayton, VIC, 3168, Australia.
Adv Healthc Mater. 2025 Apr;14(11):e2404117. doi: 10.1002/adhm.202404117. Epub 2025 Mar 20.
Ovarian cancer (OC) poses a significant clinical challenge due to its high recurrence rates and resistance to standard therapies, particularly in advanced stages where recurrence is common, and treatment is predominantly palliative. Personalized treatments, while effective in other cancers, remain underutilized in OC due to a lack of reliable biomarkers predicting clinical outcomes. Accordingly, precision medicine approaches are limited, with PARP inhibitors showing efficacy only in specific genetic contexts. Drug repurposing offers a promising, rapidly translatable strategy by leveraging existing pharmacological data to identify new treatments for OC. Patient-derived polyclonal spheroids, isolated from ascites fluid closely mimic the clinical behavior of OC, providing a valuable model for drug testing. Using these spheroids, a high-throughput drug screening pipeline capable of evaluating both cytotoxicity and anti-migratory properties of a diverse drug library, including FDA-approved, investigational, and newly approved compounds is developed. The findings highlight the importance of 3D culture systems, revealing a poor correlation between drug efficacy in traditional 2D models and more clinically relevant 3D spheroids. This approach has expedited the identification of promising candidates, such as rapamycin, which demonstrated limited activity as a monotherapy but synergized effectively with standard treatments like cisplatin and paclitaxel in vitro. In combination with platinum-based therapy, Rapamycin led to significant in vitro cytotoxicity and a marked reduction in tumor burden in a syngeneic in vivo model. This proof-of-concept study underscores the potential of drug repurposing to rapidly advance new treatments into clinical trials for OC, offering renewed hope for patients with advanced disease.
卵巢癌(OC)因其高复发率和对标准疗法的耐药性而带来重大临床挑战,尤其是在晚期,复发很常见,治疗主要是姑息性的。个性化治疗在其他癌症中有效,但在OC中由于缺乏预测临床结果的可靠生物标志物而未得到充分利用。因此,精准医学方法有限,PARP抑制剂仅在特定基因背景下显示出疗效。药物重新利用通过利用现有药理学数据来识别OC的新治疗方法,提供了一种有前景、可快速转化的策略。从腹水分离的患者来源的多克隆球体紧密模拟OC的临床行为,为药物测试提供了有价值的模型。利用这些球体,开发了一种高通量药物筛选流程,能够评估包括FDA批准、研究性和新批准化合物在内的多种药物库的细胞毒性和抗迁移特性。研究结果突出了3D培养系统的重要性,揭示了传统2D模型中的药物疗效与更具临床相关性的3D球体之间的相关性较差。这种方法加快了有前景的候选药物的识别,例如雷帕霉素,它作为单一疗法活性有限,但在体外与顺铂和紫杉醇等标准治疗有效协同。与铂类疗法联合使用时,雷帕霉素在同基因体内模型中导致显著的体外细胞毒性和肿瘤负担明显减轻。这项概念验证研究强调了药物重新利用将新治疗方法快速推进到OC临床试验的潜力,为晚期疾病患者带来了新的希望。